arXiv subjects

M. D. Ediger

Publications and source records attributed to M. D. Ediger.

22 records · Page 2Linked to original sources

arXiv2023

Two-step devitrification of ultrastable glasses

The discovery of ultrastable glasses has raised novel challenges about glassy systems. Recent experiments studied the macroscopic devitrification of ultrastable glasses into liquids upon heating but lacked microscopic resolution. We use molecular dynamics simulations to analyse the kinetics of this transformation. In the most stable systems, devitrification occurs after a very large time, but the liquid emerges in two steps. At short times, we observe the rare nucleation and slow growth of isolated droplets containing a liquid maintained under pressure by the rigidity of the surrounding glass. At large times, pressure is released after the droplets coalesce into large domains, which accelerates devitrification. This two-step process produces pronounced deviations from the classical Avrami kinetics and explains the emergence of a giant lengthscale characterising the devitrification of bulk ultrastable glasses. Our study elucidates the nonequilibrium kinetics of glasses following a large temperature jump, which differs from both equilibrium relaxation and aging dynamics, and will guide future experimental studies.

cond-mat.stat-mech↗

arXiv2022

Understanding the fragile-to-strong transition in silica from microscopic dynamics

In this work, we revisit the fragile-to-strong transition (FTS) in the simulated BKS silica from the perspective of microscopic dynamics in an effort to elucidate the dynamical behaviors of fragile and strong glass-forming liquids. Softness, which is a machine-learned feature from local atomic structures, is used to predict the microscopic activation energetics and long-term dynamics. The FTS is found to originate from a change in the temperature dependence of the microscopic activation energetics. Furthermore, results suggest there are two diffusion channels with different energy barriers in BKS silica. The fast dynamics at high temperatures is dominated by the channel with small energy barriers ($<\sim$1 eV), which is controlled by the short-range order. The rapid closing of this diffusion channel when lowering temperature leads to the fragile behavior. On the other hand, the slow dynamics at low temperatures is dominated by the channel with large energy barriers controlled by the medium-range order. This slow diffusion channel changes only subtly with temperature, leading to the strong behavior. The distributions of barriers in the two channels show different temperature dependences, causing a crossover at $\sim$3100 K. This transition temperature in microscopic dynamics is consistent with the inflection point in the configurational entropy, suggesting there is a fundamental correlation between microscopic dynamics and thermodynamics.

cond-mat.dis-nn↗

arXiv2021

Vapor deposition rate modifies anisotropic glassy structure of an anthracene-based organic semiconductor

We control the anisotropic molecular packing of vapor-deposited glasses of ABH113, a deuterated anthracene derivative with promise for future OLED materials, by changing the deposition rate and substrate temperature at which they are prepared. We find that, at substrate temperatures from 0.65Tg to 0.92Tg, deposition rate significantly modifies the orientational order in the vapor-deposited glasses as characterized by X-ray scattering and birefringence. Both measures of anisotropic order can be described by a single deposition rate-substrate temperature superposition (RTS). This supports the applicability of the surface equilibration mechanism and generalizes the RTS principle from previous model systems with liquid crystalline order to non-mesogenic organic semiconductors. We find that vapor-deposited glasses of ABH113 have significantly enhanced density and thermal stability compared to their counterparts prepared by liquid-cooling. For organic semiconductors, the results of this study provide an efficient guide for using deposition rate to prepare stable glasses with controlled molecular packing.

cond-mat.mtrl-sci↗

arXiv2013

Measurement of segmental mobility during constant strain rate deformation of a poly(methyl methacrylate) glass

We describe an apparatus for performing constant strain rate deformations of polymer glasses while simultaneously measuring the segmental mobility with an optical probe reorientation method. Poly(methyl methacrylate) glasses were deformed at Tg - 19 K, for local strain rates between 3.7x10-5/s and 1.2x10-4/s. In these experiments, the mobility initially increases in the pre-yield regime, by a factor of 40 to 160, as compared to the undeformed PMMA glass. The mobility then remains constant after yield, even as the stress is decreasing due to strain softening. This is consistent with the view that the sample is being pulled higher on the potential energy landscape in this regime. Higher strain rates lead to higher mobility in the post-yield regime and, for the range of strain rates investigated, mobility and strain rate are linearly correlated. We observe that thermal history has no influence on mobility after yield and that deformation leads to a narrowing of the distribution of segmental relaxation times. These last three observations are consistent with previously reported constant stress experiments on PMMA glasses. The experimental features reported here are compared to computer simulations and theoretical models.

cond-mat.mtrl-sci↗